<p>Quadriceps muscles from <b>(A,D)</b> vehicle control <b>(B,E)</b> rapamycin-treated or <b>(C,F)</b> chloroquine-treated animals were stained with SDH antibody to observe mitochondrial proliferation and oxidative fibers/capacity (Black arrows point to Type II dark fibers; White arrows point to lighter fibers) and <b>(G-L)</b> Oil Red O to observe lipid droplets in WT and VCP<sup><b>R155H/+</b></sup> mice at 20 months of age (Magnification: 400X). Black arrows point to increased Oil Red O Staining; white arrows point to diminished Oil Red O staining. <b>(M)</b> Quantification of Type II oxidative fibers with autophagy-modifying drugs. The number of mice analyzed per experiment is 8–10. Statistical significance is denoted by *<i>p</i><0.005...
The mitochondrial DNA A3243G mutation causes neuromuscular disease. To investigate the muscle-specif...
Mitochondrial DNA (mtDNA) mutations lead to decrements in mitochondrial function and accelerated rat...
<p>Mitochondria were isolated by differential centrifugation from the whole spinal cord of SOD1-G93A...
<p>Quadriceps muscles from <b>(A,B)</b> control, <b>(C,D)</b> rapamycin- and <b>(E,F)</b> chloroquin...
<p>(A) Oil Red O staining of WT and VCP<sup>R155H/R155H</sup> mice quadriceps reveals increased lipi...
<p>(A,B) Grip strength and Rotarod measurements analyses at 15-months of age, (C,D) H&E and (E,F) Oi...
Mutations in the valosin containing protein (VCP) gene cause hereditary Inclusion body myopathy (hIB...
Mutations in the valosin containing protein (VCP) gene cause hereditary Inclusion body myopathy (hIB...
The mTOR inhibitor rapamycin ameliorates the clinical and biochemical phenotype of mouse, worm, and ...
The vast majority of mitochondrial disorders have limited the clinical management to palliative care...
Abstract The mTOR inhibitor rapamycin ameliorates the clinical and biochemical phenotype of mouse, w...
Mitochondrial DNA (mtDNA) mutations lead to decrements in mitochondrial function and accelerated rat...
Age-induced mitochondrial DNA deletion mutations may underlie cell loss and tissue aging. Rapamycin ...
Thesis (Ph.D.)--University of Washington, 2014Treatments to stop or reverse the debilitating progres...
<p>Immunohistochemical histological analyses comparing WT and heterozygote VCP<sup><b>R155H/+</b></s...
The mitochondrial DNA A3243G mutation causes neuromuscular disease. To investigate the muscle-specif...
Mitochondrial DNA (mtDNA) mutations lead to decrements in mitochondrial function and accelerated rat...
<p>Mitochondria were isolated by differential centrifugation from the whole spinal cord of SOD1-G93A...
<p>Quadriceps muscles from <b>(A,B)</b> control, <b>(C,D)</b> rapamycin- and <b>(E,F)</b> chloroquin...
<p>(A) Oil Red O staining of WT and VCP<sup>R155H/R155H</sup> mice quadriceps reveals increased lipi...
<p>(A,B) Grip strength and Rotarod measurements analyses at 15-months of age, (C,D) H&E and (E,F) Oi...
Mutations in the valosin containing protein (VCP) gene cause hereditary Inclusion body myopathy (hIB...
Mutations in the valosin containing protein (VCP) gene cause hereditary Inclusion body myopathy (hIB...
The mTOR inhibitor rapamycin ameliorates the clinical and biochemical phenotype of mouse, worm, and ...
The vast majority of mitochondrial disorders have limited the clinical management to palliative care...
Abstract The mTOR inhibitor rapamycin ameliorates the clinical and biochemical phenotype of mouse, w...
Mitochondrial DNA (mtDNA) mutations lead to decrements in mitochondrial function and accelerated rat...
Age-induced mitochondrial DNA deletion mutations may underlie cell loss and tissue aging. Rapamycin ...
Thesis (Ph.D.)--University of Washington, 2014Treatments to stop or reverse the debilitating progres...
<p>Immunohistochemical histological analyses comparing WT and heterozygote VCP<sup><b>R155H/+</b></s...
The mitochondrial DNA A3243G mutation causes neuromuscular disease. To investigate the muscle-specif...
Mitochondrial DNA (mtDNA) mutations lead to decrements in mitochondrial function and accelerated rat...
<p>Mitochondria were isolated by differential centrifugation from the whole spinal cord of SOD1-G93A...